Brain-derived neurotrophic factor genetic polymorphism rs6265 and creativity
The protein brain-derived neurotrophic factor (BDNF) promotes neural plasticity of the central nervous system and plays an important role for learning and memory. A single nucleotide polymorphism (rs6265) at position 66 in the pro-region of the human BDNF gene, resulting in a substitution of the ami...
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description | The protein brain-derived neurotrophic factor (BDNF) promotes neural plasticity of the central nervous system and plays an important role for learning and memory. A single nucleotide polymorphism (rs6265) at position 66 in the pro-region of the human BDNF gene, resulting in a substitution of the amino acid valine (val) with methionine (met), leads to attenuated BDNF secretion and has been associated with reduced neurocognitive function. Inhomogeneous results have been found regarding the effect of the BDNF genotype on behavior. We determined the BDNF genotype and performance on the Compound Remote Associate (CRA) task as a common measure of creativity in 76 healthy university students. In our main analyses, we did not find significant differences between met-carriers (n = 30) and non-met carriers (n = 46). In a secondary analysis, we found that met-carriers had a slower solution time (medium effect size) for items of medium difficulty. Our results suggest that met-carriers and non-met-carriers do not generally differ regarding their creativity, but non-met-carriers may have a certain advantage when it comes to moderately difficult problems. The wider literature suggests that both genetic variants come with advantages and disadvantages. Future research needs to sharpen our understanding of the disadvantages and, potentially, advantages met allele carriers may have. |
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A single nucleotide polymorphism (rs6265) at position 66 in the pro-region of the human BDNF gene, resulting in a substitution of the amino acid valine (val) with methionine (met), leads to attenuated BDNF secretion and has been associated with reduced neurocognitive function. Inhomogeneous results have been found regarding the effect of the BDNF genotype on behavior. We determined the BDNF genotype and performance on the Compound Remote Associate (CRA) task as a common measure of creativity in 76 healthy university students. In our main analyses, we did not find significant differences between met-carriers (n = 30) and non-met carriers (n = 46). In a secondary analysis, we found that met-carriers had a slower solution time (medium effect size) for items of medium difficulty. Our results suggest that met-carriers and non-met-carriers do not generally differ regarding their creativity, but non-met-carriers may have a certain advantage when it comes to moderately difficult problems. The wider literature suggests that both genetic variants come with advantages and disadvantages. Future research needs to sharpen our understanding of the disadvantages and, potentially, advantages met allele carriers may have.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0291397</identifier><identifier>PMID: 37703265</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Amino acid substitution ; Amino acids ; Analysis ; Biology and Life Sciences ; Brain ; Brain-derived neurotrophic factor ; Central nervous system ; Cognition ; Colleges & universities ; Creative ability ; Creativity ; Flexibility ; Gene polymorphism ; Genetic aspects ; Genetic diversity ; Genetic polymorphisms ; Genetic variance ; Genotype & phenotype ; Health aspects ; Health risks ; Intelligence ; Medicine and Health Sciences ; Memory ; Mental depression ; Mental disorders ; Methionine ; Neural plasticity ; Nucleotides ; Physical Sciences ; Polymorphism ; Psychotherapy ; Research and Analysis Methods ; Secondary analysis ; Single-nucleotide polymorphism ; Social Sciences ; Valine</subject><ispartof>PloS one, 2023-09, Vol.18 (9), p.e0291397</ispartof><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Hertenstein et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright: © 2023 Hertenstein et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>2023 Hertenstein et al 2023 Hertenstein et al</rights><rights>2023 Hertenstein et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c619t-3cd132796553bf8c7a760ba7fcb2bd2d3e0a720645f84d401689560e66292bf03</cites><orcidid>0000-0002-1205-7157 ; 0000-0001-6467-0933 ; 0000-0002-0841-3630</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499242/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499242/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2104,2930,23873,27931,27932,53798,53800</link.rule.ids></links><search><contributor>Nasri, Amina</contributor><creatorcontrib>Hertenstein, Elisabeth</creatorcontrib><creatorcontrib>Kuhn, Marion</creatorcontrib><creatorcontrib>Landmann, Nina</creatorcontrib><creatorcontrib>Maier, Jonathan-Gabriel</creatorcontrib><creatorcontrib>Schneider, Carlotta Louisa</creatorcontrib><creatorcontrib>Fehér, Kristoffer Daniel</creatorcontrib><creatorcontrib>Frase, Lukas</creatorcontrib><creatorcontrib>Riemann, Dieter</creatorcontrib><creatorcontrib>Feige, Bernd</creatorcontrib><creatorcontrib>Nissen, Christoph</creatorcontrib><title>Brain-derived neurotrophic factor genetic polymorphism rs6265 and creativity</title><title>PloS one</title><description>The protein brain-derived neurotrophic factor (BDNF) promotes neural plasticity of the central nervous system and plays an important role for learning and memory. A single nucleotide polymorphism (rs6265) at position 66 in the pro-region of the human BDNF gene, resulting in a substitution of the amino acid valine (val) with methionine (met), leads to attenuated BDNF secretion and has been associated with reduced neurocognitive function. Inhomogeneous results have been found regarding the effect of the BDNF genotype on behavior. We determined the BDNF genotype and performance on the Compound Remote Associate (CRA) task as a common measure of creativity in 76 healthy university students. In our main analyses, we did not find significant differences between met-carriers (n = 30) and non-met carriers (n = 46). In a secondary analysis, we found that met-carriers had a slower solution time (medium effect size) for items of medium difficulty. Our results suggest that met-carriers and non-met-carriers do not generally differ regarding their creativity, but non-met-carriers may have a certain advantage when it comes to moderately difficult problems. The wider literature suggests that both genetic variants come with advantages and disadvantages. Future research needs to sharpen our understanding of the disadvantages and, potentially, advantages met allele carriers may have.</description><subject>Amino acid substitution</subject><subject>Amino acids</subject><subject>Analysis</subject><subject>Biology and Life Sciences</subject><subject>Brain</subject><subject>Brain-derived neurotrophic factor</subject><subject>Central nervous system</subject><subject>Cognition</subject><subject>Colleges & universities</subject><subject>Creative ability</subject><subject>Creativity</subject><subject>Flexibility</subject><subject>Gene polymorphism</subject><subject>Genetic aspects</subject><subject>Genetic diversity</subject><subject>Genetic polymorphisms</subject><subject>Genetic variance</subject><subject>Genotype & phenotype</subject><subject>Health aspects</subject><subject>Health risks</subject><subject>Intelligence</subject><subject>Medicine and Health Sciences</subject><subject>Memory</subject><subject>Mental 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Kristoffer Daniel</au><au>Frase, Lukas</au><au>Riemann, Dieter</au><au>Feige, Bernd</au><au>Nissen, Christoph</au><au>Nasri, Amina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain-derived neurotrophic factor genetic polymorphism rs6265 and creativity</atitle><jtitle>PloS one</jtitle><date>2023-09-13</date><risdate>2023</risdate><volume>18</volume><issue>9</issue><spage>e0291397</spage><pages>e0291397-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The protein brain-derived neurotrophic factor (BDNF) promotes neural plasticity of the central nervous system and plays an important role for learning and memory. A single nucleotide polymorphism (rs6265) at position 66 in the pro-region of the human BDNF gene, resulting in a substitution of the amino acid valine (val) with methionine (met), leads to attenuated BDNF secretion and has been associated with reduced neurocognitive function. Inhomogeneous results have been found regarding the effect of the BDNF genotype on behavior. We determined the BDNF genotype and performance on the Compound Remote Associate (CRA) task as a common measure of creativity in 76 healthy university students. In our main analyses, we did not find significant differences between met-carriers (n = 30) and non-met carriers (n = 46). In a secondary analysis, we found that met-carriers had a slower solution time (medium effect size) for items of medium difficulty. Our results suggest that met-carriers and non-met-carriers do not generally differ regarding their creativity, but non-met-carriers may have a certain advantage when it comes to moderately difficult problems. The wider literature suggests that both genetic variants come with advantages and disadvantages. Future research needs to sharpen our understanding of the disadvantages and, potentially, advantages met allele carriers may have.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>37703265</pmid><doi>10.1371/journal.pone.0291397</doi><tpages>e0291397</tpages><orcidid>https://orcid.org/0000-0002-1205-7157</orcidid><orcidid>https://orcid.org/0000-0001-6467-0933</orcidid><orcidid>https://orcid.org/0000-0002-0841-3630</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acid substitution Amino acids Analysis Biology and Life Sciences Brain Brain-derived neurotrophic factor Central nervous system Cognition Colleges & universities Creative ability Creativity Flexibility Gene polymorphism Genetic aspects Genetic diversity Genetic polymorphisms Genetic variance Genotype & phenotype Health aspects Health risks Intelligence Medicine and Health Sciences Memory Mental depression Mental disorders Methionine Neural plasticity Nucleotides Physical Sciences Polymorphism Psychotherapy Research and Analysis Methods Secondary analysis Single-nucleotide polymorphism Social Sciences Valine |
title | Brain-derived neurotrophic factor genetic polymorphism rs6265 and creativity |
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